Source: FDA, document on fileFDA released the Form 483 itself. The document linked above is our copy of FDA's file, stored by us so the link cannot break, and FDA's own copy is linked beside it.
To check this against FDA, open FDA's record for this establishment on FDA's Data Dashboard, which lists this inspection under FEI 3008723337.
RX South DBA RX3 Compounding Pharmacy LLC
Chester, Virginia, United States
Issue DateOctober 29, 2015
FEI Number3008723337
CountryUnited States
Status
No Warning Letter
Product Type
Drugs
Establishment Type
Producer of Sterile Drug Products
RX South DBA RX3 Compounding Pharmacy LLC FDA Form 483, Chester, Virginia, October 29, 2015
